Status: current, Primitive. Date: 31-Jul 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2920595018 | Gilberts syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
46000010 | Gilbert's syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
46001014 | Gilbert-Lereboullet syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
46002019 | Familial nonhemolytic bilirubinemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
46003012 | Chronic intermittent juvenile jaundice | en | Synonym | Active | Case insensitive | SNOMED CT core |
46004018 | Constitutional hepatic dysfunction | en | Synonym | Active | Case insensitive | SNOMED CT core |
46005017 | Cholemia familiaris simplex | en | Synonym | Active | Case insensitive | SNOMED CT core |
46006016 | Familial nonhemolytic jaundice | en | Synonym | Active | Case insensitive | SNOMED CT core |
46007013 | Gilbert's disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
46008015 | Hereditary nonhemolytic jaundice | en | Synonym | Active | Case insensitive | SNOMED CT core |
46009011 | Benign unconjugated bilirubinemia syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
46010018 | Meulengracht syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
46011019 | Low-grade chronic hyperbilirubinemia syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
46012014 | Congenital familial cholemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
483557015 | Benign unconjugated bilirubinaemia syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
483558013 | Congenital familial cholaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
483559017 | Cholaemia familiaris simplex | en | Synonym | Active | Case insensitive | SNOMED CT core |
483560010 | Gilbert syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
483561014 | Familial nonhaemolytic bilirubinaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
483562019 | Hereditary nonhaemolytic jaundice | en | Synonym | Active | Case insensitive | SNOMED CT core |
483563012 | Familial nonhaemolytic jaundice | en | Synonym | Active | Case insensitive | SNOMED CT core |
483564018 | Low-grade chronic hyperbilirubinaemia syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
758078013 | Gilbert's syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Gilbert's syndrome | Finding site | Body system structure | false | Inferred relationship | Some | ||
Gilbert's syndrome | Is a | Hyperbilirubinaemia | false | Inferred relationship | Some | ||
Gilbert's syndrome | Is a | Inherited disorder of bilirubin metabolism | true | Inferred relationship | Some | ||
Gilbert's syndrome | Is a | Congenital anomaly of liver | false | Inferred relationship | Some | ||
Gilbert's syndrome | Is a | Digestive system hereditary disorder | false | Inferred relationship | Some | ||
Gilbert's syndrome | Finding site | Digestive organ structure | false | Inferred relationship | Some | 1 | |
Gilbert's syndrome | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 1 | |
Gilbert's syndrome | Finding site | Liver structure | false | Inferred relationship | Some | ||
Gilbert's syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Dubin-Johnson syndrome | Is a | False | Gilbert's syndrome | Inferred relationship | Some | |
Neonatal jaundice with Gilbert's syndrome | Associated with | True | Gilbert's syndrome | Inferred relationship | Some | 1 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set